ClinVar Miner

List of variants reported as uncertain significance for language disorder by OMIM

Included ClinVar conditions (10):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_016256.4(NAGPA):c.982C>T (p.Arg328Cys)	rs139526942	0.00062
NM_016256.4(NAGPA):c.252C>G (p.His84Gln)	rs755458782	0.00049

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